A combined platform for testing fireproof materials for cables includes a main frame for providing operating space; an air circulation system including a fresh air supply unit for supplying fresh air into the operating space and an exhaust gas treatment unit for treating the gas in the operating space under set conditions; an open flame system for providing an open flame for testing cables; a water circulation system for supplying water at least to the exhaust gas treatment unit and the operating space; and a control system for collecting at least the temperature and gas concentration in the operating space, and performing process control based on the collected results. The actual working conditions of scenarios such as fire-resistant cable tunnels and fire-resistant cable trenches can be simulated, and multiple tests such as combustion performance test and physical and chemical performance test can be carried out under various working conditions.

A combined platform for testing fireproof materials for cables includes a main frame for providing operating space; an air circulation system including a fresh air supply unit for supplying fresh air into the operating space and an exhaust gas treatment unit for treating the gas in the operating space under set conditions; an open flame system for providing an open flame for testing cables; a water circulation system for supplying water at least to the exhaust gas treatment unit and the operating space; and a control system for collecting at least the temperature and gas concentration in the operating space, and performing process control based on the collected results. The actual working conditions of scenarios such as fire-resistant cable tunnels and fire-resistant cable trenches can be simulated, and multiple tests such as combustion performance test and physical and chemical performance test can be carried out under various working conditions.

Provided are a total organic carbon measurement method and a total organic carbon measurement device capable of determining whether or not an acid has been added to a sample. An acid is introduced into a reaction unit in which the sample is placed from a reservoir in which the acid is reserved (step S103). The conductivity of the sample into which the acid has been introduced is measured (step S105). The introduction of the acid from the reservoir into the reaction unit is detected on the basis of a change in the conductivity of the sample (step S107).

The present invention provides a method for forming a history of natural gas accumulation by using carbon isotopes by a pyrolysis experiment. The method includes: obtaining activation energy distribution and a frequency factor of light carbon methane; carrying out carbon isotope kinetics simulation of natural gas in a study area by using a spreadsheet function of Excel to obtain activation energy, a mass fraction and a frequency factor of heavy carbon methane; establishing a burial history and a thermal history of the study area based on geological data; and combining the activation energy distribution and frequency factor of the heavy carbon methane with the burial history and thermal history of the study area, and establishing an instantaneous curve, a cumulative curve and a stage cumulative curve of natural gas under geological conditions on a geologic time scale.

The present invention provides a method for forming a history of natural gas accumulation by using carbon isotopes by a pyrolysis experiment. The method includes: obtaining activation energy distribution and a frequency factor of light carbon methane; carrying out carbon isotope kinetics simulation of natural gas in a study area by using a spreadsheet function of Excel to obtain activation energy, a mass fraction and a frequency factor of heavy carbon methane; establishing a burial history and a thermal history of the study area based on geological data; and combining the activation energy distribution and frequency factor of the heavy carbon methane with the burial history and thermal history of the study area, and establishing an instantaneous curve, a cumulative curve and a stage cumulative curve of natural gas under geological conditions on a geologic time scale.

The analyzing apparatus includes a reactor, a detector, a carrier gas supplier, a carrier gas flow rate adjustor, a flow control program memory, and a flow rate controller. The detector communicates with an internal space of the reactor, and detects a target substance generated by reaction of a specific component in the internal space. The carrier gas supplier supplies, to the internal space, carrier gas for transporting the target substance generated in the internal space. The carrier gas flow rate adjustor adjusts a carrier gas flow rate supplied from the carrier gas supplier to the internal space. The flow control program memory stores a flow control program set to increase the carrier gas flow rate during measurement from the process of introduction of a sample into the internal space to the process of detection of the target substance by the detector.

The analyzing apparatus includes a reactor, a detector, a carrier gas supplier, a carrier gas flow rate adjustor, a flow control program memory, and a flow rate controller. The detector communicates with an internal space of the reactor, and detects a target substance generated by reaction of a specific component in the internal space. The carrier gas supplier supplies, to the internal space, carrier gas for transporting the target substance generated in the internal space. The carrier gas flow rate adjustor adjusts a carrier gas flow rate supplied from the carrier gas supplier to the internal space. The flow control program memory stores a flow control program set to increase the carrier gas flow rate during measurement from the process of introduction of a sample into the internal space to the process of detection of the target substance by the detector.

An elemental analysis device includes a first electrode and a second electrode between which a crucible MP containing a sample is nipped, and that heats the sample. The second electrode includes a second electrode main body that has a tip end having a substantially cylindrical shape, a second electrode tip, a cap that nips the second electrode tip between the cap and the second electrode main body such that a part of the second electrode tip is exposed to an outside, and a second screwing structure that includes a male thread and a female thread provided between the second electrode main body and the cap, and the second screwing structure further includes a purge groove that extends in a pitch direction and that is provided as a cutout provided to a part of crests of a thread of at least one of the male thread and the female thread.

An elemental analysis device includes a first electrode and a second electrode between which a crucible MP containing a sample is nipped, and that heats the sample. The second electrode includes a second electrode main body that has a tip end having a substantially cylindrical shape, a second electrode tip, a cap that nips the second electrode tip between the cap and the second electrode main body such that a part of the second electrode tip is exposed to an outside, and a second screwing structure that includes a male thread and a female thread provided between the second electrode main body and the cap, and the second screwing structure further includes a purge groove that extends in a pitch direction and that is provided as a cutout provided to a part of crests of a thread of at least one of the male thread and the female thread.

An element analysis method is capable of maintaining accuracy of zero-point correction equivalent to that in the related art while shortening the time required for element analysis. The method includes heating a sample placed in a crucible in a heating furnace, and measuring an amount of an element contained in a gas discharged from the heating furnace by an analysis mechanism to analyze the element contained in the sample. The method includes: a blank measurement step of measuring the amount of the element contained in the gas discharged from the heating furnace when only the crucible is heated; and a step of setting an amount of zero-point correction based on a measurement value in a transient state region where the measurement value rises in blank data obtained in the blank measurement step.